Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
RxRecalls Get alerts

National Drug Code

Is NDC 0941-0424-52 recalled?

DIANEAL Low Calcium with Dextrose · 2000 mL in 1 BAG (0941-0424-52)

Yes — this exact package was recalled

1 FDA recall names the code 0941-0424-52 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.

Active ingredient
sodium chloride, sodium lactate, calcium chloride, magnesium chloride and dextrose
Strength
DEXTROSE MONOHYDRATE 1.5 g/100mL; SODIUM CHLORIDE 538…
Form
Injection, Solution · Intraperitoneal
Labeler
Vantive US Healthcare LLC
Type
Human Prescription Drug
Product code
0941-0424

Recalls naming this package

Class II · Moderate risk

Dianeal Low Calcium

Lack of Assurance of Sterility: Confirmed customer complaints for leaks on the tubing.

Terminated Sterility / contamination Baxter Healthcare Corporation NDC 0941-0424-52 D-0351-2019

Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.

Other recalled products from this labeler